Correction to: Nature Communications; https://doi.org/10.1038/s41467-018-06014-6; published online 05 November 2018.
The original version of this Article contained an error in the spelling of the author Laurence Faivre, which was incorrectly given as Laurence Faive. This has now been corrected in both the PDF and HTML versions of the Article.
Author information
These authors contributed equally: Lot Snijders Blok, Justine Rousseau, Joanna Twist.
These authors jointly supervised this work: Simon E. Fisher, Philippe M. Campeau.
Authors and Affiliations
Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands
Lot Snijders Blok, Stefan Lelieveld, Rolph Pfundt, Sandra Jansen, Tjitske Kleefstra & Han G. Brunner
Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands
Lot Snijders Blok, Pelagia Deriziotis & Simon E. Fisher
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands
Lot Snijders Blok, Sandra Jansen, Tjitske Kleefstra, Han G. Brunner & Simon E. Fisher
CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada
Justine Rousseau, Sophie Ehresmann & Philippe M. Campeau
National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA
Joanna Twist, Motoki Takaku, Cat Taylor, John D. Roberts, Robert M. Petrovich & Paul A. Wade
Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands
Hanka Venselaar
Division of Genetics and Genomics, Boston Children’s Hospital, Boston, MA, 02115, USA
Lance H. Rodan, Catherine B. Nowak & Jessica Douglas
Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA
Kathryn J. Swoboda
Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA
Marcie A. Steeves & Inderneel Sahai
Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands
Connie T. R. M. Stumpel, Alexander P. A. Stegmann & Han G. Brunner
Nemours Childrens Clinic, Orlando, FL, 32827, USA
Patricia Wheeler
Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA
Marcia Willing & Elise Fiala
Valley Children’s Hospital, Madera, CA, 93636, USA
Aaina Kochhar
British Columbia Children’s Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada
William T. Gibson, Ana S. A. Cohen & Ruky Agbahovbe
Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada
William T. Gibson, Ana S. A. Cohen & Ruky Agbahovbe
Department of Medical Genetics and Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada
A. Micheil Innes & P. Y. Billie Au
Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK
Julia Rankin
Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA
Ilse J. Anderson
Greenwood Genetic Center, Greenwood, SC, 29646, USA
Steven A. Skinner, Raymond J. Louie & Hannah E. Warren
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France
Alexandra Afenjar
AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France
Boris Keren, Caroline Nava & Julien Buratti
Groupe de Recherche Clinique (GRC) ‘déficience intellectuelle et autisme’ UPMC, Paris, 75005, France
Boris Keren & Caroline Nava
INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France
Caroline Nava
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases “Nord/Est/Ile-de-France”, FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France
Arnaud Isapof
GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France
Diana Rodriguez
Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA
Raymond Lewandowski & Jennifer Propst
Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands
Ton van Essen
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea
Murim Choi & Sangmoon Lee
Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children’s Hospital, Seoul, 08826, Republic of Korea
Jong H. Chae
Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK
Susan Price
GeneDx, Gaithersburg, MD, 20877, USA
Rhonda E. Schnur, Ganka Douglas & Ingrid M. Wentzensen
Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany
Christiane Zweier & André Reis
Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA
Martin G. Bialer & Christine Moore
Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands
Marije Koopmans, Eva H. Brilstra, Glen R. Monroe, Koen L. I. van Gassen & Ellen van Binsbergen
University Hospitals Bristol, Department of Clinical Genetics, St Michael’s Hospital, Bristol, BS2 8EG, UK
Ruth Newbury-Ecob & Lucy Bownass
Department of Clinical Genetics, University Children’s Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria
Ingrid Bader
Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria
Johannes A. Mayr & Saskia B. Wortmann
Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany
Saskia B. Wortmann
Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany
Saskia B. Wortmann
Communication Sciences and Disorders, Augustana College, Rock Island, IL, 61201, USA
Kathy J. Jakielski
Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA
Edythe A. Strand
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany
Katja Kloth & Tatjana Bierhals
Waseda University, Tokyo, 169-8050, Japan
Shinichi Machida & Hitoshi Kurumizaka
Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté, Dijon, 21070, France
Laurence Faivre, Julien Thevenon & Mirna Assoum
Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d’Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France
Laurence Faivre, Julien Thevenon & Mirna Assoum
Waisman Center, Phonology Project, Madison, WI, 53705-2280, USA
Lawrence Shriberg
Sainte-Justine Hospital, University of Montreal, Montreal, QC, H3T 1C5, Canada
Philippe M. Campeau
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK
Jeremy F. McRae, Stephen Clayton, Tomas W. Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Nadia Akawi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones, Daniel King, Netravathi Krishnappa, Laura E. Mason, Tarjinder Singh, Adrian R. Tivey, Jana Awada, A. Paul Bevan, Simon Brent, Elena Chatzimichali, Irina Colgiu, Irina Colgiu, Dylan de Vries, Emma Gray, Philip Greene, Susan Gribble, Liu He, Lucy Hildyard, Ben Hutton, Rosemary Kelsell, Anna Middleton, Daniel Perrett, Martin Pollard, Raheleh Rahbari, Josh Randall, Ganesh Jawahar Swaminathan, Parthiban Vijayarangakannan, Sara Widaa, Emily Wilkinson, Helen V. Firth, Caroline F. Wright, David R. FitzPatrick, Jeffrey C. Barrett & Matthew E. Hurles
MRC Human Genetics Unit, MRC IGMM, University of Edinburgh, Western General Hospital, Edinburgh, EH4 2XU, UK
Stuart Aitken, Andrew Jackson, Wayne Lam, Anne Lampe, Eddy Maher, David Moore & David R. FitzPatrick
Department of Engineering Science, University of Oxford, Parks Road, Oxford, OX1 3PJ, UK
Mohsan Alvi
Wessex Clinical Genetics Service, University Hospital Southampton, Princess Anne Hospital, Coxford Road, Southampton, SO16 5YA, UK
Munaza Ahmed, Diana Baralle, David J. Bunyan, Amanda Collins, Morag N. Collinson, Amanda Collins, Morag N. Collinson, Nicola Foulds, Lucy Harrison, Victoria Harrison, Katherine Lachlan, I. Karen Temple, Audrey Torokwa & Diana Wellesley
Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Odstock Road, Salisbury, Wiltshire, SP2 8BJ, UK
Munaza Ahmed, Diana Baralle, David J. Bunyan, Amanda Collins, Morag N. Collinson, Amanda Collins, Morag N. Collinson, Nicola Foulds, Lucy Harrison, Victoria Harrison, Katherine Lachlan, I. Karen Temple, Audrey Torokwa & Diana Wellesley
Faculty of Medicine, University of Southampton, Building 85, Life Sciences Building, Highfield Campus, Southampton, SO17 1BJ, UK
Munaza Ahmed, Diana Baralle, David J. Bunyan, Amanda Collins, Morag N. Collinson, Amanda Collins, Morag N. Collinson, Nicola Foulds, Lucy Harrison, Victoria Harrison, Katherine Lachlan, I. Karen Temple, Audrey Torokwa & Diana Wellesley
South West Thames Regional Genetics Centre, St George’s Healthcare NHS Trust, St George’s, University of London, Cranmer Terrace, London, SW17 0RE, UK
Uruj Anjum, Frances Elmslie, Tessa Homfray, Sahar Mansour, Karen Marks, Meriel McEntagart, Anand Saggar, Kate Tatton-Brown & Rohan Taylor
Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff, CF14 4XW, UK
Hayley Archer, Angus Clarke, Sally Davies, Karenza Evans, Andrew Fry, Dhavendra Kumar, Sian Morgan, Hood Mugalaasi, Annie Procter, Julian Sampson & Vinod Varghese
Department of Clinical Genetics, Block 12, Glan Clwyd Hospital, Rhyl, Denbighshire, LL18 5UJ, UK
Hayley Archer, Angus Clarke, Sally Davies, Karenza Evans, Andrew Fry, Dhavendra Kumar, Sian Morgan, Hood Mugalaasi, Annie Procter, Julian Sampson & Vinod Varghese
East Anglian Medical Genetics Service, Box 134, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK
Ruth Armstrong, Simon Holden, Sarju Mehta, Soo-Mi Park, Joan Paterson, Lucy Raymond, Jonathan Roberts, Richard Sandford, Ingrid Simonic, Marc Tischkowitz, Becky Treacy, Sarah Wallwark, Sarah Wilcox, Geoff Woods & Helen V. Firth
Sheffield Regional Genetics Services, Sheffield Children’s NHS Trust, Western Bank, Sheffield, S10 2TH, UK
Meena Balasubramanian, Stuart Ingram, Diana Johnson, Louise Nevitt, Michael J. Parker, Oliver Quarrell, Emma Shearing & Kath Smith
Manchester Centre for Genomic Medicine, St Mary’s Hospital, Central Manchester University Hospitals NHSFoundation Trust, Manchester Academic Health Science Centre, Manchester, M13 9WL, UK
Siddharth Banka, Kate Chandler, Jill Clayton-Smith, Jill Clayton-Smith, Yanick Crow, Dian Donnai, Carina Donnelly, Sofia Douzgou, Lorraine Gaunt, Elizabeth Jones, Bronwyn Kerr, Helen Kingston, Kay Metcalfe, Emma Miles, Helen Murphy & Zara Skitt
North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, Great Ormond Street Hospital, Great Ormond Street, London, WC1N3JH, UK
Angela Barnicoat, Maria Bitner-Glindzicz, Kate Brunstrom, Georgina Hollingsworth, Jane Hurst, Lucy Jenkins, V. K. Ajith Kumar, Melissa Lees, Alison Male, Elisabeth Rosser, Richard Scott, Jonathon Waters & Louise Wilson
North of Scotland Regional Genetics Service, NHS Grampian, Department of Medical Genetics Medical School, Foresterhill, Aberdeen, AB25 2ZD, UK
Paul Batstone, Mariella D’Alessandro, John Dean, Ruth McGowan, Catherine McWilliam, Zosia Miedzybrodzka, Alison Ross & Shalaka Samant
East of Scotland Regional Genetics Service, Human Genetics Unit, Pathology Department, NHS Tayside, Ninewells Hospital, Dundee, DD1 9SY, UK
David Baty, Jonathan Berg, David Goudie, Norman Pratt, Debbie Rice & Susann Schweiger
Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Department of Clinical Genetics, Chapel Allerton Hospital, Chapeltown Road, Leeds, LS7 4SA, UK
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Edward Blair, Deirdre Cilliers, Susan Clasper, Richard Gibbons, Usha Kini, Andrea Nemeth, Julie Phipps, Joanna Poulton, Abigail Pridham, Hellen Purnell, Anneke Seller, Debbie Shears & Helen Stewart
West Midlands Regional Genetics Service, Birmingham Women’s NHS Foundation Trust, Birmingham Women’s Hospital, Edgbaston, Birmingham, B15 2TG, UK
David Bohanna, Trevor Cole, Nicola Cooper, Helen Cox, Trevor Cole, Nicola Cooper, Helen Cox, Lily Islam, Joanna Jarvis, Gail Kirby, Derek Lim, Kirsten McKay, Dominic J. McMullan, Jenny Morton, Swati Naik, Andrew Norman, Kai-Ren Ong, Chirag Patel, Nicola Ragge, Saba Sharif, Mark Tein, Julie Vogt & Denise Williams
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Northern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust, Belfast City Hospital, Lisburn Road, Belfast, BT9 7AB, UK
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Peninsula Clinical Genetics Service, Royal Devon and Exeter NHS Foundation Trust, Clinical Genetics Department, Royal Devon & Exeter Hospital (Heavitree), Gladstone Road, Exeter, EX1 2ED, UK
Carole Brewer, Bruce Castle, Gemma Devlin, Sian Ellard, Sarah Everest, Emma Kivuva, Charles Shaw-Smith, Claire Turner, Peter Turnpenny & Carolyn Tysoe
South East Thames Regional Genetics Centre, Guy’s and St Thomas’ NHS Foundation Trust, Guy’s Hospital, Great Maze Pond, London, SE1 9RT, UK
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Leicestershire Genetics Centre, University Hospitals of Leicester NHS Trust, Leicester Royal Infirmary (NHS Trust), Leicester, LE1 5WW, UK
Lara Cresswell, Lara Cresswell, Beckie Kaemba, Sandra Kazembe & Pradeep Vasudevan
Nottingham Regional Genetics Service, City Hospital Campus, Nottingham University Hospitals NHS Trust, The Gables, Hucknall Road, Nottingham, NG5 1PB, UK
Gareth Cross, Gareth Cross, Abhijit Dixit, Jacqueline Eason, Rachel Harrison, Katherine Martin, Ajoy Sarkar, Ann Selby, Nora Shannon & Mohnish Suri
West of Scotland Regional Genetics Service, NHS Greater Glasgow and Clyde, Institute of Medical Genetics, Yorkhill Hospital, Glasgow, G3 8SJ, UK
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Bristol Genetics Service (Avon, Somerset, Gloucs and West Wilts), University Hospitals Bristol NHS Foundation Trust, St Michael’s Hospital, St Michael’s Hill, Bristol, BS2 8DT, UK
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National Centre for Medical Genetics, Our Lady’s Children’s Hospital, Crumlin, Dublin 12, Ireland
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Department of Clinical Genetics, Block 12, Glan Clwyd Hospital, Rhyl, Denbighshire, LL18 5UJ, Wales, UK
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Nuffield Department of Obstetrics & Gynaecology, University of Oxford, Level 3, Women’s Centre, John Radcliffe Hospital, Oxford, OX3 9DU, UK
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Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Old Road Campus Research Building, Oxford, OX3 7DQ, UK
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Big Data Institute, University of Oxford, Roosevelt drive, Oxford, OX3 7LF, UK
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The DDD study
- Jeremy F. McRae
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Corresponding authors
Correspondence to Simon E. Fisher or Philippe M. Campeau.
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Blok, L.S., Rousseau, J., Twist, J. et al. Author Correction: CHD3 helicase ___domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nat Commun 10, 883 (2019). https://doi.org/10.1038/s41467-019-08800-2
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DOI: https://doi.org/10.1038/s41467-019-08800-2
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